The Type VI Secretion System Encoded in Salmonella Pathogenicity Island 19 Is Required for Salmonella enterica Serotype Gallinarum Survival within Infected Macrophages

被引:52
作者
Blondel, Carlos J. [1 ]
Jimenez, Juan C. [1 ]
Leiva, Lorenzo E. [1 ]
Alvarez, Sergio A. [1 ]
Pinto, Bernardo I. [1 ]
Contreras, Francisca [1 ]
Pezoa, David [1 ]
Santiviago, Carlos A. [1 ]
Contreras, Ines [1 ]
机构
[1] Univ Chile, Dept Bioquim & Biol Mol, Fac Ciencias Quim & Farmaceut, Santiago, Chile
关键词
DYNAMICS FOLLOWING INFECTION; PSEUDOMONAS-AERUGINOSA; SEROVAR TYPHIMURIUM; GENE-EXPRESSION; ESCHERICHIA-COLI; PROTEIN SECRETION; GROWTH-PHASE; HOST-CELLS; MOLECULAR CHARACTERIZATION; AEROMONAS-HYDROPHILA;
D O I
10.1128/IAI.01165-12
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Salmonella enterica serotype Gallinarum is the causative agent of fowl typhoid, a disease characterized by high morbidity and mortality that causes major economic losses in poultry production. We have reported that S. Gallinarum harbors a type VI secretion system (T6SS) encoded in Salmonella pathogenicity island 19 (SPI-19) that is required for efficient colonization of chicks. In the present study, we aimed to characterize the SPI-19 T6SS functionality and to investigate the mechanisms behind the phenotypes previously observed in vivo. Expression analyses revealed that SPI-19 T6SS core components are expressed and produced under in vitro bacterial growth conditions. However, secretion of the structural/secreted components Hcp1, Hcp2, and VgrG to the culture medium could not be determined, suggesting that additional signals are required for T6SS-dependent secretion of these proteins. In vitro bacterial competition assays failed to demonstrate a role for SPI-19 T6SS in interbacterial killing. In contrast, cell culture experiments with murine and avian macrophages (RAW264.7 and HD11, respectively) revealed production of a green fluorescent protein-tagged version of VgrG soon after Salmonella uptake. Furthermore, infection of RAW264.7 and HD11 macrophages with deletion mutants of SPI-19 or strains with genes encoding specific T6SS core components (clpV and vgrG) revealed that SPI-19 T6SS contributes to S. Gallinarum survival within macrophages at 20 h postuptake. SPI-19 T6SS function was not linked to Salmonella-induced cytotoxicity or cell death of infected macrophages, as has been described for other T6SS. Our data indicate that SPI-19 T6SS corresponds to a novel tool used by Salmonella to survive within host cells.
引用
收藏
页码:1207 / 1220
页数:14
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